Role of gut bacterial and non-bacterial microbiota in alcohol-associated liver disease: Molecular mechanisms, biomarkers, and therapeutic prospective.


Journal

Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521

Informations de publication

Date de publication:
15 Sep 2022
Historique:
received: 16 05 2022
revised: 20 06 2022
accepted: 28 06 2022
pubmed: 6 7 2022
medline: 27 7 2022
entrez: 5 7 2022
Statut: ppublish

Résumé

Alcohol-associated liver disease (ALD) comprises a spectrum of liver diseases that include: steatosis to alcohol-associated hepatitis, cirrhosis, and ultimately hepatocellular carcinoma. The pathophysiology and potential underlying mechanisms for alcohol-associated liver disease are unclear. Moreover, the treatment of ALD remains a challenge. Intestinal microbiota include bacteria, fungi, and viruses, that are now known to be important in the development of ALD. Alcohol consumption can change the gut microbiota and function leading to liver disease. Given the importance of interactions between intestinal microbiota, alcohol, and liver injury, the gut microbiota has emerged as a potential biomarker and therapeutic target. This review focuses on the potential mechanisms by which the gut microbiota may be involved in the pathogenesis of ALD and explains how this can be translated into clinical management. We discuss the potential of utilizing the gut microbiota signature as a biomarker in ALD patients. Additionally, we present an overview of the prospect of modulating the intestinal microbiota for the management of ALD.

Identifiants

pubmed: 35787997
pii: S0024-3205(22)00460-X
doi: 10.1016/j.lfs.2022.120760
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

120760

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Nima Zafari (N)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Mahla Velayati (M)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Mostafa Fahim (M)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Mina Maftouh (M)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Ghazaleh Pourali (G)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Majid Khazaei (M)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Mohammadreza Nassiri (M)

Recombinant Proteins Research Group, The Research Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad, Iran.

Seyed Mahdi Hassanian (SM)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran; Basic Sciences Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Majid Ghayour-Mobarhan (M)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Gordon A Ferns (GA)

Brighton & Sussex Medical School, Division of Medical Education, Falmer, Brighton, Sussex BN1 9PH, UK.

Mohammad Ali Kiani (MA)

Department of Pediatrics, Akbar Hospital, Mashhad University of Medical Sciences, Mashhad, Iran; Department of Pediatric Gastroenterology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Amir Avan (A)

Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran; Basic Sciences Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran; Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. Electronic address: avana@mums.ac.ir.

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Classifications MeSH